Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Saturday, September 14, 2024

Switching off ageing: People could live up to 25 per cent longer in better health if a redundant gene is switch off, according to Imperial College London. Kath Hudson reports

 Do you have a competent? doctor and hospital that will ensure further testing occurs?

Switching off ageing

People could live up to 25 per cent longer in better health if a redundant gene is switch off, according to Imperial College London. Kath Hudson reports

Research from Imperial College London indicates that switching off a protein could lead to people living up to 25 per cent longer and enjoying better health in their later years.

Back in 2017, Imperial College discovered that the protein interleukin 11 (IL-11) plays a key role in the scarring process which causes heart, kidney and liver failure, so inhibiting the gene can prevent fibrosis – the build-up of excessive connective tissue in organs – which contributes to organ failure.

Further research has shown that switching off the gene could have more far-reaching health benefits and the potential to delay many of the issues that come with ageing, including the loss of vision, hearing, hair and muscle, as well as improving lung function and metabolism, reducing the incidences of cancer and significantly adding to healthy lifespan.

Increasing healthspan and lifespan
This research is also exciting because so far the indications are showing that inhibiting this gene could extend healthspan as well as lifespan.

Professor Stuart Cook, from the Medical Research Council Laboratory of Medical Science, Imperial College – who led the research – says: “These findings are very exciting. Previously proposed life-extending drugs and treatments have either had poor side-effect profiles, or don’t work in both sexes, or could extend life, but not healthy life. However this does not appear to be the case for IL-11.”

Interleukins are proteins involved in relaying signals between the cells and help regulate cell growth, differentiation and movement. They’re important for immune responses, inflammation and fibrosis. However, IL-11, is believed to be an evolutionary hangover for humans: while it’s vital for limb regeneration in some animal species, it’s thought to be largely redundant in humans.

More interleukin 11 means faster ageing
After the age of 55, increasing levels of IL-11 are produced and previous research has linked this to chronic inflammation, fibrosis in organs, metabolism disorders, muscle wasting, frailty and cardiac fibrosis.

Clinical trials of anti IL-11 therapy are currently in the early stages for treating fibrotic lung disease and may provide a translational opportunity to determine the effects of IL-11 inhibition on ageing pathologies in older people. Early trial data suggests the intervention is safe.

In the future there is the possibility of a therapeutic drug being given in later life, or – more controversially – gene editing at birth.

The research was published in Nature and partly funded by the Medical Research Council.

More: www.hcmmag.com/interleukin

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